Disease | dementia |
Phenotype | C0085084|motor neuron disease |
Sentences | 9 |
PubMedID- 23445572 | We believe the results indicate a subgroup of motor neuron disease with dementia whose initial symptoms involve pseudobulbar palsy and dementia, and which shows rapid progression to mutism. |
PubMedID- 22300873 | The findings indicate that c9orf72 mutations cause some but not all cases of frontotemporal dementia with motor neuron disease. |
PubMedID- 21298310 | We described the cases of two patients with dementia associated with motor neuron disease, the former with frontotemporal dementia (ftd) and the latter with alzheimer's disease (ad), studied by the pittsburgh compound b-positron emission tomography (pib-pet). |
PubMedID- 21569259 | Our observations further support the concept that tdp-43 proteinopathies represent a spectrum of disorders, where preferential localization of pathogenetic inclusions and neuronal cell loss defines clinical phenotypes ranging from frontotemporal dementia with or without motor neuron disease, to corticobasal syndrome and to a progressive supranuclear palsy-like syndrome. |
PubMedID- 22051030 | Right temporal variant frontotemporal dementia with motor neuron disease. |
PubMedID- 20627585 | Comment on "semantic dementia combined with motor neuron disease". |
PubMedID- 21624986 | Predicting survival in frontotemporal dementia with motor neuron disease. |
PubMedID- 21029204 | Semantic dementia with lower motor neuron disease showing ftld-tdp type 3 pathology (sensu mackenzie). |
PubMedID- 20500451 | Ubiquitin-positive tau-negative intraneuronal inclusions in dementia with motor neuron disease: the 50th anniversary of japanese society of neuropathology. |
Page: 1